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硫内酯霉素,一种新型抗生素。III. 体外抗菌活性。

Thiolactomycin, a new antibiotic. III. In vitro antibacterial activity.

作者信息

Noto T, Miyakawa S, Oishi H, Endo H, Okazaki H

出版信息

J Antibiot (Tokyo). 1982 Apr;35(4):401-10. doi: 10.7164/antibiotics.35.401.

Abstract

Thiolactomycin is a new broad-spectrum antibiotic, active in vitro against many species of Gram-positive cocci, Enterobacteriaceae, Haemophilus, acid-fast bacteria and anaerobic bacteria. However, the activity is generally moderate and bacteriostatic in action. This antibiotic eludes cross resistance with any of the known antibacterial drugs such as ampicillin, carbenicillin or cycloserine. The effect on Gram-negative bacilli in vitro is little affected by the inoculum size, the presence of horse serum, the pH of the medium or the type of medium. When thiolactomycin was added to the assay medium, the minimum inhibitory concentration of ampicillin against inducible beta-lactamase producing strains of Staphylococcus aureus and Pseudomonas aeruginosa was reduced. Thiolactomycin inhibited the production of inducible beta-lactamase in several organisms.

摘要

硫乳霉素是一种新型广谱抗生素,在体外对多种革兰氏阳性球菌、肠杆菌科细菌、嗜血杆菌、抗酸菌和厌氧菌具有活性。然而,其活性一般中等,作用为抑菌。这种抗生素与任何已知抗菌药物如氨苄西林、羧苄西林或环丝氨酸均无交叉耐药性。体外对革兰氏阴性杆菌的作用几乎不受接种量、马血清的存在、培养基的pH值或培养基类型的影响。当将硫乳霉素添加到测定培养基中时,氨苄西林对金黄色葡萄球菌和铜绿假单胞菌的可诱导β-内酰胺酶产生菌株的最低抑菌浓度降低。硫乳霉素在几种生物体中抑制可诱导β-内酰胺酶的产生。

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